Reaction Details |
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Target | Methionine aminopeptidase 2 |
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Ligand | BDBM47468 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_957169 (CHEMBL2378707) |
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EC50 | >100000±n/a nM |
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Citation | Zhang, F; Bhat, S; Gabelli, SB; Chen, X; Miller, MS; Nacev, BA; Cheng, YL; Meyers, DJ; Tenney, K; Shim, JS; Crews, P; Amzel, LM; Ma, D; Liu, JO Pyridinylquinazolines selectively inhibit human methionine aminopeptidase-1 in cells. J Med Chem56:3996-4016 (2013) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Methionine aminopeptidase 2 |
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Name: | Methionine aminopeptidase 2 |
Synonyms: | Initiation factor 2-associated 67 kDa glycoprotein | MAP 2 | MAP2_HUMAN | METAP2 | MNPEP | MetAP 2 | Methionine aminopeptidase 2 (MetAP2) | Methionine aminopeptidases (HsMetAP2) | P67EIF2 | Peptidase M 2 | p67 |
Type: | Enzyme |
Mol. Mass.: | 52884.45 |
Organism: | Homo sapiens (Human) |
Description: | P50579 |
Residue: | 478 |
Sequence: | MAGVEEVAASGSHLNGDLDPDDREEGAASTAEEAAKKKRRKKKKSKGPSAAGEQEPDKES
GASVDEVARQLERSALEDKERDEDDEDGDGDGDGATGKKKKKKKKKRGPKVQTDPPSVPI
CDLYPNGVFPKGQECEYPPTQDGRTAAWRTTSEEKKALDQASEEIWNDFREAAEAHRQVR
KYVMSWIKPGMTMIEICEKLEDCSRKLIKENGLNAGLAFPTGCSLNNCAAHYTPNAGDTT
VLQYDDICKIDFGTHISGRIIDCAFTVTFNPKYDTLLKAVKDATNTGIKCAGIDVRLCDV
GEAIQEVMESYEVEIDGKTYQVKPIRNLNGHSIGQYRIHAGKTVPIVKGGEATRMEEGEV
YAIETFGSTGKGVVHDDMECSHYMKNFDVGHVPIRLPRTKHLLNVINENFGTLAFCRRWL
DRLGESKYLMALKNLCDLGIVDPYPPLCDIKGSYTAQFEHTILLRPTCKEVVSRGDDY
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BDBM47468 |
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n/a |
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Name | BDBM47468 |
Synonyms: | MLS000769840 | N-(2-phenylethyl)-2-(2-pyridinyl)-4-quinazolinamine | N-(2-phenylethyl)-2-pyridin-2-yl-quinazolin-4-amine | N-(2-phenylethyl)-2-pyridin-2-ylquinazolin-4-amine | Phenethyl-(2-pyridin-2-yl-quinazolin-4-yl)-amine | SMR000434573 | cid_937982 | phenethyl-[2-(2-pyridyl)quinazolin-4-yl]amine |
Type | Small organic molecule |
Emp. Form. | C21H18N4 |
Mol. Mass. | 326.3944 |
SMILES | C(Cc1ccccc1)Nc1nc(nc2ccccc12)-c1ccccn1 |
Structure |
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